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NCT00908583 · ClinicalTrials.gov registry record · Phase 4

Desensitization in Kidney Transplantation

A Phase 4 study, sponsored by University of Cincinnati.

Completed
Registry status
Phase 4
Development phase
44
Enrollment target

NCT00908583: Completed Phase 4 study, sponsored by University of Cincinnati.

NCT00908583 is a Phase 4 study that has completed, run by University of Cincinnati. The registered enrollment target is 44 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00908583, a Phase 4 study, has completed, sponsored by University of Cincinnati.

COMPLETED
Registry status
Phase 4
Development phase
44 participants
Enrollment target

Study Summary

To determine if deletional strategies will provide effective desensitization.

Primary Outcome

Number of living donor transplant candidates who convert to a negative flow T- and B-cell crossmatch via desensitization and are subsequently transplanted

Interventions

  • DRUG Rituximab
  • DRUG Methylprednisolone
  • DRUG Bortezomib
  • DRUG plasmapheresis

Trial Details

FieldValue
Enrollment Target 44 participants
Start Date 2009-05
Est. Completion 2012-11
Phase Phase 4
University of Cincinnati

245 total trials

What the finished NCT00908583 record still lists

NCT00908583 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 4 interventions - of which Rituximab is the first listed.

NCT00908583 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00908583 about?

NCT00908583 is a clinical study titled "Desensitization in Kidney Transplantation". To determine if deletional strategies will provide effective desensitization.

What is the current status of trial NCT00908583?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 44 participants. The study started on 2009-05. Estimated completion is 2012-11.

What interventions are being tested in trial NCT00908583?

The interventions under investigation include: Rituximab (DRUG), Methylprednisolone (DRUG), Bortezomib (DRUG), plasmapheresis (DRUG).

Who is sponsoring clinical trial NCT00908583?

This trial is sponsored by University of Cincinnati, which has 245 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00908583's enrollment target sits among peer trials

44 1363rd of 2000 higher than 630 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00908583, the US trial registry maintained by the National Library of Medicine. NCT00908583 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.